Arrowhead Research

Manager, Clinical Supply Management

Arrowhead Research$135K — $155K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 4-year college degree in a relevant discipline preferred
  • Experience with electronic interactive response technologies for inventory management
  • Experience managing supply for clinical investigations of injectables and biologics
  • Solid vendor management skills
  • Thorough understanding of GMP, GCP, and ICH standards

Responsibilities

  • Collaborate cross-functionally to execute IMP supply planning and management
  • Develop and manage clinical supplies distribution plans for clinical studies
  • Coordinate clinical supplies forecasting to ensure timely availability
  • Serve as the primary contact for clinical supplies planning and inventory monitoring
  • Align IMP release testing and stability with program milestones
  • Develop SOPs and processes for clinical supplies management
  • Act as a subject matter expert on labeling and packaging options

Benefits

  • Competitive salary
  • Excellent benefit package
  • Opportunity to work in a dynamic and innovative environment
  • Collaborative work culture with cross-functional teams
  • Focus on developing novel therapies for patients with intractable diseases
Full Job Description
The Position

This function is responsible for coordination of investigational medicinal product (IMP) and ancillary supply planning, forecasting, labeling, packaging, distribution, inventory monitoring, and reconciliation for Arrowhead Pharmaceuticals clinical development programs.

This role is based in onsite with an expectation to be in the office five days a week.

Responsibilities
  • Collaborate cross-functionally with Clinical Development, Manufacturing, Regulatory Affairs, and Quality Assurance to plan and execute IMP supply planning including labeling and packaging, utilization forecasting, inventory control, and international shipments and external depot management for Phase 1-4 international clinical studies
  • Develop clinical supplies distribution plans based on program and study timelines, trial design, recruitment, geography, and manufacturing schedules
  • Coordinate and manage clinical supplies forecasting and utilization to ensure on-time and reliable availability of IMP and required ancillary supplies in support of study execution
  • Serve as the primary point of contact cross-functionally for clinical supplies planning, inventory monitoring, and distribution, and third-party service provider/depot selection and oversight
  • Coordinate with Manufacturing Operations, Quality Assurance and Regulatory Affairs to ensure planned IMP release testing/re-testing, stability, expiry dates, labeling and packaging schedules align with program milestones, adjusting as necessary over the course of the program
  • Develop and manage SOPs, work instructions, processes, systems, and forms governing clinical supplies management in alignment with industry standards and regulatory requirements
  • Serve as internal subject matter expert on fit-for-purpose labeling and packaging design options best suited to meet study requirements
  • Serve as liaison between Clinical Operations and Quality Assurance to manage IMP stability parameters, temperature deviation management, product complaints and associated investigations

Requirements
  • 4-year college degree (relevant discipline preferred)
  • Experience with electronic interactive response technologies for inventory management
  • Experience with managing supply for clinical investigations of injectables and biologics
  • Solid vendor management skills
  • Ability to proactively perform and complete duties with minimal supervision in an accurate and timely manner
  • Thorough understanding of GMP, GCP, and ICH standards governing IMP labeling, packaging, and distribution
  • Proficient in MS Officer (Word, Excel, and PowerPoint)
  • Ability to work in a team or independently
  • Effective interpersonal, written, and verbal communication skills
  • Able to critically evaluate and prioritize job tasks and the impact on overall study execution
  • Strong problem-solving capabilities
  • Effectively collaborates with Study Team members
  • Exceptional organizational skills with the ability to multi-task and prioritize
  • Attention to detail
  • Ability to work with distributed team members and outside vendors

Preferred

  • Experience in multiple therapeutic areas


Wisconsin pay range

$120,000-$140,000 USD

California pay range

$135,000-$155,000 USD

Arrowhead provides competitive salaries and an excellent benefit package.

Candidates must have current, valid authorization to work in the country where this role is located.

California Applicant Privacy Policy

About Arrowhead Research

Arrowhead Research is a biotechnology company that develops RNA interference (RNAi) therapeutics. The company was founded in 2007 and is headquartered in Pasadena, California. Arrowhead's RNAi technology targets specific genes to silence their expression, which can be used to treat a variety of diseases. The company's pipeline includes treatments for liver disease, cancer, and cardiovascular disease. Arrowhead has partnerships with pharmaceutical companies such as Amgen and Janssen Pharmaceuticals. The company has received FDA approval for some of its products and is conducting clinical trials for others.
Learn more about Arrowhead Research
Size
329 employees
Market Cap
$4 billion
Industry
Net Income
-$102.6 million
Founded
2004
5 Year Trend
+50.6%
Revenue
$79.8 million
NASDAQ

Similar Jobs

More Jobs at Arrowhead Research

More Pharmaceuticals & Biotech Jobs

Find similar Manager, Clinical Supply Management jobs: